Canonical Allele Identifier: CA391621912

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634169T>C (hg19) ; chr15:g.34341968T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341968T>C , CM000677.2:g.34341968T>C	GRCh38
NC_000015.9:g.34634169T>C , CM000677.1:g.34634169T>C	GRCh37
NC_000015.8:g.32421461T>C	NCBI36
NG_007951.1:g.1097A>G , LRG_270:g.1097A>G
NG_011562.1:g.6194A>G , LRG_345:g.6194A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*26A>G	ENSP00000453475.1:n.*26A>G
ENST00000699926.1:c.198A>G	ENSP00000514692.1:p.Ter66Trp
ENST00000699934.1:c.159+36A>G	ENSP00000514697.1:n.159+36A>G
ENST00000699935.1:c.219A>G	ENSP00000514698.1:p.Ter73Trp
ENST00000699936.1:c.129A>G	ENSP00000514699.1:p.Ter43Trp
ENST00000699937.1:c.180A>G	ENSP00000514700.1:p.Ter60Trp
ENST00000699938.1:c.159+36A>G	ENSP00000514701.1:n.159+36A>G
ENST00000699939.1:n.342A>G
ENST00000328848.6:c.195A>G MANE Select	ENSP00000332198.5:p.Ter65Trp
ENST00000328848.5:c.195A>G	ENSP00000332198.4:p.Ter65Trp
ENST00000557912.1:c.*26A>G	ENSP00000453475.1:n.*26A>G
NM_018648.3:c.195A>G , LRG_345t1:c.195A>G	NP_061118.1:p.Ter65Trp
NM_018648.4:c.195A>G MANE Select	NP_061118.1:p.Ter65Trp